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GENATLAS PHENOTYPE

last update : 03-12-2015

Symbol	CWS3
Location	11q23.1
Name	Cowden syndrome 3
Corresponding gene	SDHD
Main clinical features	hamartomatous polyps of the gastrointestinal tract, mucocutaneous lesions, and increased risk of developing neoplasms multiple hamartomatous lesions, especially of the skin, mucous membranes, breast and thyroid, are encountered; verrucous skin lesions of the face and limbs, cobblestone-like papules of the gingiva and buccal mucosa, and multiple facial trichilemmomas
Genetic determination
Function/system disorder
Type	disease

Remark(s)